Table 1

Genomic instability and tumour growth for YAMC clones and control cell lines

Treatment, cell lines and subclonesNumber of treatments*Cells with aneuploidy and tetraploidy (%±SD)†Tumour size (mm3)IHC staining for keratins‡Histopathology of tumours
Untreated
 HCT116NoneND1751+Poorly differentiated carcinoma
 YAMC1010.6±3.5
Treated with 4-hydroxy-2-nonenal
 H11023.8
 H21024.261+Poorly differentiated carcinoma
 H31013.2, 11.830Acute/chronic inflammation
 H41030.5±4.7
 H51016.1±4.9201+Poorly differentiated carcinoma
 H61022.6
 H71033.8±9.2195+Poorly differentiated carcinoma
 H81018.9, 24.4
 H8-1840.7±13.9
 H8-4890.8
 H91026.9, 16.6
Exposed to Enterococcus faecalis-infected macrophages
 37M10-11017.5±8.7
 37M10-31022.8, 38.054Lymphoid mass
 37M10-51077.0±13.5
 37M10-61031.1±13.3
 37M10-71077.3
 M3108.462+Poorly differentiated carcinoma
 M1110ND584+Poorly differentiated carcinoma invading skin
 M1210ND
 M1310ND661+Poorly differentiated carcinoma
 M141084.9±19.3
 M151032.3±8.41117+Poorly differentiated carcinoma invading skin
 M161021.3
 M171030.174+Poorly differentiated carcinoma invading muscle
 M6-1633.4
  • *YAMC cells were fed twice a week and subcultured once a week for 10 successive weeks.

  • †Average and SD calculated for experiments repeated ≥3 times. For experiments with <3 repeats, percentages listed for each individual experiment.

  • ‡See materials and methods for immunohistochemical (IHC) staining using a pan-keratin reagent.

  • ND, not determined; +, positive staining in cancer cell cytoplasm; –, negative staining.